Synthesis, Antitubercular and Anticancer Activities of Substituted Furyl-quinazolin-3(4H)-ones
作者:Nulgulmnalli M. Raghavendra、Parameshwaran Thampi、Purvarga M. Gurubasavarajaswamy、Dharmarajan Sriram
DOI:10.1002/ardp.200700096
日期:2007.12
Some novel substituted‐3‐[(1E)‐(substituted‐2‐furyl)‐methylene]amino}quinazolin‐4(3H)‐one (5, 6, 7) a–f were synthesized by a multi‐step process. These synthesized compounds are characterized by various spectroscopic techniques and evaluated for their antitubercular and anticancer activities. Biological activity indicated that some of the title compounds are potent antitubercular and anticancer agents
通过多步法合成了一些新的取代-3-[(1E)-(取代-2-呋喃基)-亚甲基]氨基}喹唑啉-4(3H)-one(5,6,7)a-f . 这些合成的化合物通过各种光谱技术进行表征,并评估了它们的抗结核和抗癌活性。生物活性表明,一些标题化合物是有效的抗结核和抗癌剂。